{{Rsnum
|rsid=755109
|Gene=HEMGN
|Chromosome=9
|position=97933921
|Orientation=plus
|GMAF=0.2649
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=HEMGN
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 18.9 | 45.0 | 36.0
| HCB | 2.9 | 26.3 | 70.8
| JPT | 0.9 | 18.0 | 81.1
| YRI | 1.4 | 19.9 | 78.8
| ASW | 5.3 | 24.6 | 70.2
| CHB | 2.9 | 26.3 | 70.8
| CHD | 0.9 | 36.4 | 62.6
| GIH | 6.9 | 30.7 | 62.4
| LWK | 1.8 | 24.5 | 73.6
| MEX | 13.8 | 36.2 | 50.0
| MKK | 8.3 | 28.8 | 62.8
| TSI | 21.6 | 43.1 | 35.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19197348
|Trait=Quantitative traits
|Title=Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
|RiskAllele=C
|Pval=0.000001
|OR=0.31
|ORtxt=[NR] mIU/L decrease
|OA=1
}}

Thyroid-stimulating hormone being the quantitative trait associated with in {{PMID|19197348|OA=1
}}

{{PMID Auto
|PMID=22493691
|Title=Novel associations for hypothyroidism include known autoimmune risk loci.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs755109
|overall_frequency_n=38
|overall_frequency_d=128
|overall_frequency=0.296875
|n_genomes=25
|n_genomes_annotated=0
|n_haplomes=33
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}